Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pgen.1000218
DC Field | Value | |
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dc.title | Genetic association and expression studies indicate a role of Toll-like receptor 8 in pulmonary tuberculosis | |
dc.contributor.author | Davila S. | |
dc.contributor.author | Hibberd M.L. | |
dc.contributor.author | Dass R.H. | |
dc.contributor.author | Wong H.E.E. | |
dc.contributor.author | Sahiratmadja E. | |
dc.contributor.author | Bonnard C. | |
dc.contributor.author | Alisjahbana B. | |
dc.contributor.author | Szeszko J.S. | |
dc.contributor.author | Balabanova Y. | |
dc.contributor.author | Drobniewski F. | |
dc.contributor.author | Van Crevel R. | |
dc.contributor.author | Van De Vosse E. | |
dc.contributor.author | Nejentsev S. | |
dc.contributor.author | Ottenhoff T.H.M. | |
dc.contributor.author | Seielstad M. | |
dc.date.accessioned | 2019-11-06T09:37:13Z | |
dc.date.available | 2019-11-06T09:37:13Z | |
dc.date.issued | 2008 | |
dc.identifier.citation | Davila S., Hibberd M.L., Dass R.H., Wong H.E.E., Sahiratmadja E., Bonnard C., Alisjahbana B., Szeszko J.S., Balabanova Y., Drobniewski F., Van Crevel R., Van De Vosse E., Nejentsev S., Ottenhoff T.H.M., Seielstad M. (2008). Genetic association and expression studies indicate a role of Toll-like receptor 8 in pulmonary tuberculosis. PLoS Genetics 4 (10) : e1000218. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pgen.1000218 | |
dc.identifier.issn | 15537390 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/161682 | |
dc.description.abstract | Despite high rates of exposure, only 5-10% of people infected with Mycobacterium tuberculosis will develop active tuberculosis (TB) disease, suggesting a significant role for genetic variation in the human immune response to this infection. Here, we studied TB association and expression of 18 genes involved in the Toll-like receptor (TLR) pathways. Initially, we genotyped 149 sequence polymorphisms in 375 pulmonary TB patients and 387 controls from Indonesia. We found that four polymorphisms in the TLR8 gene on chromosome X showed evidence of association with TB susceptibility in males, including a non-synonymous polymorphism rs3764880 (Met1Val; P = 0.007, odds ratio (OR) = 1.8, 95% c.i. = 1.2-2.7). We genotyped these four TLR8 polymorphisms in an independent collection of 1,837 pulmonary TB patients and 1,779 controls from Russia and again found evidence of association in males (for rs3764880 P = 0.03, OR = 1.2, 95% c.i. = 1.02-1.48). Combined evidence for association is P = 1.2×10-3-6×10-4. In addition, a quantitative PCR analysis indicated that TLR8 transcript levels are significantly up-regulated in patients during the acute phase of disease (P = 9.3661025), relative to baseline levels following successful chemotherapy. A marked increase in TLR8 protein expression was also observed directly in differentiated macrophages upon infection with M. bovis bacille Calmette-Guérin (BCG). Taken together, our results provide evidence, for the first time, of a role for the TLR8 gene in susceptibility to pulmonary TB across different populations. © 2008 Davila et al. | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20191101 | |
dc.subject | toll like receptor 8 | |
dc.subject | messenger RNA | |
dc.subject | TLR8 protein, human | |
dc.subject | adolescent | |
dc.subject | adult | |
dc.subject | aged | |
dc.subject | article | |
dc.subject | controlled study | |
dc.subject | DNA polymorphism | |
dc.subject | female | |
dc.subject | gene expression | |
dc.subject | gene sequence | |
dc.subject | genetic analysis | |
dc.subject | genetic susceptibility | |
dc.subject | human | |
dc.subject | lung tuberculosis | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | Mycobacterium tuberculosis | |
dc.subject | nucleotide sequence | |
dc.subject | polymerase chain reaction | |
dc.subject | single nucleotide polymorphism | |
dc.subject | X chromosome | |
dc.subject | case control study | |
dc.subject | cell line | |
dc.subject | gene frequency | |
dc.subject | gene linkage disequilibrium | |
dc.subject | genetic predisposition | |
dc.subject | genetics | |
dc.subject | haplotype | |
dc.subject | immunology | |
dc.subject | Indonesia | |
dc.subject | metabolism | |
dc.subject | middle aged | |
dc.subject | sexual development | |
dc.subject | Mycobacterium tuberculosis | |
dc.subject | Adolescent | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Aged, 80 and over | |
dc.subject | Case-Control Studies | |
dc.subject | Cell Line | |
dc.subject | Chromosomes, Human, X | |
dc.subject | Female | |
dc.subject | Gene Expression | |
dc.subject | Gene Frequency | |
dc.subject | Genetic Predisposition to Disease | |
dc.subject | Haplotypes | |
dc.subject | Humans | |
dc.subject | Indonesia | |
dc.subject | Linkage Disequilibrium | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Polymorphism, Single Nucleotide | |
dc.subject | RNA, Messenger | |
dc.subject | Sex Characteristics | |
dc.subject | Toll-Like Receptor 8 | |
dc.subject | Tuberculosis, Pulmonary | |
dc.type | Article | |
dc.contributor.department | SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH | |
dc.description.doi | 10.1371/journal.pgen.1000218 | |
dc.description.sourcetitle | PLoS Genetics | |
dc.description.volume | 4 | |
dc.description.issue | 10 | |
dc.description.page | e1000218 | |
Appears in Collections: | Elements Staff Publications |
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